| Literature DB >> 27843114 |
Abdelbasset A Farahat1, Cheree Bennett-Vaughn2, Ekaterina M Mineva2, Arvind Kumar2, Tanja Wenzler3, Reto Brun3, Yang Liu2, W David Wilson2, David W Boykin2.
Abstract
A series of novel benzimidazole diamidines were prepared from the corresponding dicyano analogues either by applying Pinner methodology (5a-c, 10 and 13a) or by making amidoximes intermediates that were reduced to the corresponding amidines (15a-c). The new amidines were evaluated in vitro against the protozoan parasite Trypanosoma brucei rhodesiense (T. b. r.). The thiophene analogue 5b and the N-methyl compound 15a showed superior antitrypanosomal activity compared to that of the parent I. Published by Elsevier Ltd.Entities:
Keywords: Antitrypanosomal activity; Benzimidazole diamidines; DAPI; DNA minor groove binders
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Year: 2016 PMID: 27843114 DOI: 10.1016/j.bmcl.2016.11.006
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823